The internet is a safe haven for people to act nasty, but it is also representative of cultural opinion at large. Based on this knowledge, I am extraordinarily dismayed that with all the PSA’s for Lyme Disease and new info circulating around it, it still doesn’t “count” as a serious illness to many people.
Of course all the details about my late stage neurological Lyme, like how I had fibromyalgia so bad I couldn’t move my limbs for a spell, were cut from Chopped, and the CO poisoning was played up because it made me look insane that a stove tried to kill me. The reactions from people, though, were still shocking: I didn’t have cancer, how could I call myself a survivor? My illnesses didn’t compare to cancer. The other two contestants had cancer, and I need to GET OVER MYSELF. Never mind that my CO poisoning– which I have very real blood work and medical records from, just like my Lyme– involved a diagnosis of Alzheimer’s by a Cedars Sinai neurologist, and the gas killed my ex’s cat, it was considered “trite” compared to cancer.
Lyme disease has a tendency to keep people laid up for years, and many simply never get well. There is no “cure,” only methods of treatment that very thankfully work for some, like me. My family and I did intensive research to find holistic treatments for both my illnesses when they each occurred, and thankfully, I successfully moved past both. My mom had cancer, and was mortified when I told her yesterday about people’s statements of my illnesses being “nothing” compared. Pain and suffering are pain and suffering, and one thing that can kill you is no less bad than another thing that can kill you.
There is simply no need, ever, to compare illnesses and minimize the suffering of others. People used the hashtag “#killerstoves” to mock my experience as minimal compared to cancer. Some even said there is no way it happened, because I’d be dead, which is clearly untrue: the ventilation problem was real, and was fixed by real HVAC people. The exposure was slow and low and not detectable on an alarm designed to only detect life threatening levels. It left me with a huge array of brain damage related troubles, all of which I have recovered from fully via holistic methods. (And most definitely NOT only with avocados, that was some fun editing.)
Our culture is rife with judgment, and social media fuels our ability to depersonalize others. We are all critics from our couches. I write this not to say I feel I was perceived unfairly (that’s a whole different blog!), but to ask people to realize that being laid up for years is a nightmare, whether or not one is sick with cancer. Period.
Besides, you know, affecting people’s lives positively and stuff, my recent speech for the Lyme Angeles Lyme disease group has gotten me to finally remember how to spell the word e-x-c-e-r-p-t. It’s one of my only spelling nemeses, and I’ve had to use it repeatedly when posting clips (aka excerpts) from my speech. Now I’m confident that I can spell it in my sleep. I’m equally confident that you will learn something from at least one of these three video clips from my speech! =)
Just because you can put it in your body, doesn’t mean you should
Let’s talk sugar, sugar
I hope you have hope
The will to survive is powerful, but there is something inside us that dwells in a far more important place than survival alone does. Survival is a start, but to be alive does not mean to be well. There is something inside us that I’ve begun to think of as the Recovery Molecule.
I’m starting to consider myself an expert at getting, and then healing naturally from, weird and controversial illnesses. Lyme Disease is gaining momentum in terms of recognition, but this past year my little family suffered from slow chemical poisoning in our home for six months, and every doctor I saw for it was befuddled. Few people survive carbon monoxide poisoning, and no research is generally done for it because there are no drugs to cure it. From winter to summer, I had severe joint pain. And for a full year, until December 2012, I lost my sense of presence, my memory, and my overall ability to think clearly. Being in my head was absolute hell. I couldn’t remember what I did from moment to moment, I couldn’t empathize with anyone, I couldn’t even handle simple addition or subtraction.
In about a month, the same amount of time it took me to catapult into wellness from Lyme, my brain recovered. (Incidentally, it was the month of December, same as Lyme, only two years later.) I utilized different modules than with Lyme, this time being helped by camel milk, lymphatic drainage massage, a supplement called Mag-Mind, and a seriously copious daily consumption of avocados, one of the best brain foods. I’ve pretty much recovered from the poisoning now, save for my metabolism refusing to return all the way and let me be as skinny as I was before this past year, but that is a minimal problem.
There is an instinct to survive, for sure. But during my times of illness, I WAS surviving. And, to be honest, it didn’t count for all that much. I’m the first one to acknowledge that when ill, I’m not exactly a positive person. People constantly said I’d be fine, I’d get over it, I would triumph, and it mostly just made me angry. They couldn’t *feel* how terrible my situation was, they didn’t understand, who were they to claim I’d be ok when I felt like life would be easier if I were dead? But there was a piece of me, far inside beyond my grumbling and complaining, that believed them. And that belief, I believe, is the Recovery Molecule. That kernel of hope so far inside, you can hardly sense it when you’re chronically ill, is as powerful as love itself. And everybody knows, thanks to Hollywood and Disney and reality, that there is pretty much nothing more powerful than love.
I don’t know if it’s love for ourselves, or those we’re close to, or what, that provides that kernel of hope. I just know that if you can picture it, and feel it, and focus on it, and freaking just BELIEVE a tiny little bit that you can be ok again, you CAN. I’ve gotten there twice now, from states that were deemed irrecoverable by professionals. And I did it without ANY pharmaceuticals. At different times I’ve been offered everything from Doxycycline to Adderall to Cymbalta to Ketamine. Screw the drugs. Screw the doctors pushing them, telling you you can’t get better without them. Make Mr. Google your best friend and do all the research you can on alternative therapies, then heal yourself better than any doctor ever could.
Thanks to my YouTube interview from Blythe Raw Live, as well as word of mouth, I get emails regularly asking for advice on how to recover from Lyme. I send people to my blogs with my protocols, and I offer any words of wisdom I can come up with at the time. But it never feels like enough, like I can do enough to save anyone else from the pain and horror of serious illness, and I want to be able to do more. This is the best I can do, sharing this idea of a Recovery Molecule. Please find yours inside. Please tune in as hard as you can to your deepest self, and find that thought that you could be ok. You will be better than ok. You will be so much wiser for having gone through this. It seems impossible, but illness is an enormous gift. It teaches us gratitude in a way we could never experience otherwise. My ability to think clearly again is a gift. Being able to breathe without pain is a gift. Find your gifts, stop waging war against your body, and make friends with your Recovery Molecule. It works, and I am proof. I am a happy, able-bodied, clear-thinking symbol of recovery, and you can be too.
PLEASE NOTE: Due to the volume of inquiries I receive requesting help for Lyme Disease, I am unable to reply to all blog comments and emails. If you are interested in scheduling a phone or Skype consultation with me on treating Lyme Disease naturally, please contact me directly by email or phone.
So far, I’ve had Lyme Disease and Bartonella in complete remission for 4 years, and that includes having spent 6-8 months minimum getting seriously exposed to carbon monoxide. If one can get hardcore chronic CO poisoning and still not relapse, I think it’s safe to say their treatment system was damn successful. In total, I dealt with Lyme for about 2 1/2 years before getting it into remission, which is shorter than many people out there, but still long enough for it to have taken over my body on a cellular level. At my worst, I had fibromyalgia so bad that my legs would not bend enough for me to walk.
I have a document that I’ve sent to many people with everything I did to get well, and decided it was time to post it here for the interwebs at large to have access to. Some things are more personal than I’d really care to share publicly, but I am doing so for the sake of hoping to help others. Note that this is just what worked for ME, and is not medical advice from a professional. I’m just a health foodie chef girl who manages to survive an array of wacky illnesses and wants to share whatever possible to help others recover too.
Lyme Success- What I Did:
-The #1 thing that killed the Lyme was a GB 4000 rife machine. It costs about $2500, my parents bought it for me. Basically, it is a
radio frequency machine that bursts both the lyme and the cysts the disease creates inside your cells to protect itself from being killed.
(Antibiotics make the lyme build stronger and stronger cyst protections, which is why people plateau so quickly on them.) I also
found useful the rife’s programs/settings for pain, detox, etc. A cheaper option is a doug coil, which can be homemade, or a Hulda Clark Zapper. Though the cost of the GB 4000 is high, it is cheaper than antibiotics and all their supplies, and much more effective.
-Therapy helped a lot with the entire process. Lyme eats up your brain and creates whacked out, f-ed up emotional problems; I would sit in the closet in the dark and cry for hours, with no cause or understanding of why. I’d always been pretty stable before, that
wasn’t normal for me at all and was very scary. I also had a LOT of awful suicidal thoughts that came as soon as any conflict arose in
life. I just couldn’t deal with anything without feeling overwhelmed and like I wanted to die. Therapy not only got rid of all that, it
gave me hope that I would get better, which in turn, I did. I did DNMS, developmental needs meeting strategy, along with EMDR, eye movement desensitization reprocessing. My therapist taught me how to be sick, and then, how to be a better version of myself when I got well.
-Supplements are VITAL. I took daily all of the following: sarsaparilla root, pau d’arco, chlorella, milk thistle, probiotics, proteolytic enzymes, zeolite, krill oil, olive leaf, magnesium, immunity mushroom blend, ubiquinol, and a multiple with high amounts of b/c/d etc. plus an antioxidant blend.
-Acupuncture was the thing that actually catapulted me into wellness. I had already killed the lyme, but was so overrun with toxins I couldn’t get out that I hadn’t yet felt any recovery. Acupuncture, specifically the mobile cupping, mobilized the toxins out, and I began recovering the day in late December 2010 that I first had it done.
-Coffee enemas. I know, major wtf. But seriously, they helped a lot. There is pretty much NO way you can get out all the toxins building up from killing lyme without drastic actions. Google has all the info on how the caffeine stimulates your liver to dump the toxins out. I did these twice a week, minimum.
-Epsom salt baths with hydrogen peroxide, after every rife treatment. They help pull the toxins out through your skin.
-Diet. I’ve always been an extreme health foodie, but I had to go as far as cutting out all grains, fruit, etc. for awhile. Lyme makes bad
stuff grow in your intestines, and both ibs and candida are very common in Lyme patients, so you can’t feed the yeast or it makes the
Lyme stronger by creating a more acidic internal environment. Incidentally, I had horrific ibs before being diagnosed and fixed both
that and the major candida symptoms with a product called Intestinew by Renew Life. Organic, unprocessed food is key.
-Kombucha. I drank 16-32 oz a day, which is pricey, but it’s the only thing that ever helped me palpably feel better, plus it’s full of
-E3 Live: again, pricey. It’s a good way to get high potency greens, but I didn’t feel it really helped until I was already on the way to
-For insomnia, they gave me ketamine, to which I said no way. I managed to sleep with large doses of amantilla, which is valerian root
extract, and a chinese herbal complex called an shui wan.
-For pain, a topical cream called Thermoderm provided substantial relief. It’s cheap. Also, pot helped with pain, specifically pot with
a low thc to high cannabanoid ratio.
As for what to avoid:
-Lyme disease forums on which everyone is still ill. Majorly depressing.
-Antibiotics if possible, which only have a 65% recovery rate and a 35% relapse rate anyway and will likely ruin one’s digestive system indefinitely. They are the standard course of treatment.
-Cowden Protocol, or herbs from it. The herx (die off reaction) is the worst ever… like bugs crawling all over you, bad drug trip, tear
your eyes out, bad. This includes samento, cumanda, and the other herbal antimicrobials. The herbs with it like burbur, pinella,
magnesium malate, and serrapeptase are fine.
The Number One Lesson That Helped Me:
In my interview with the fabulous Blythe of Blythe Raw Live, I detailed my process with Lyme, as well as the statement from my therapist that was utterly transformational to my healing process. The Lyme clip is only about five minutes total and has some good info, but if you don’t want to watch it all, fast forward to about four minutes in for that part. I think it’s the most powerful when spoken. You can watch it here.
Again, I’m no professional! I grew up in a very holistic household that taught me to always choose natural remedies before Western Medicine when possible. In my opinion and experience, that is the smartest, most productive, and best way to go for overall health.
Maybe it’s the anticipation that the all-too-brief cherry season is about to hit, but I’ve been on a major kick with dried and frozen cherries lately. I am loving the “black forest” flavor of cherries and chocolate, as evidenced by my last blog for cookie dough balls. While I always try to incorporate as many detoxing and antioxidant rich foods into my diet, that’s especially important now, as I’ve recently embarked on a healing journey from chronic carbon monoxide poisoning. I’m doing hyperbaric oxygen therapy, and it forces toxins out of your cells as it forces oxygen into them. Unfortunately, even though I have my Chronic Lyme Disease in remission, it still inhibits my body’s ability to detox, so toxins being pushed into my system = me feeling even worse. Therefore I am embracing antioxidant and detoxifying foods with extra vigor… but of course I still want them to taste good. With this smoothie, I’ve combined red kale with organic frozen cherries, protein, and cacao powder into a shake that tastes more “dessert” than “detox.”
Note that while I’m big on drinking smoothies, I am less big on making them, and I like to use a lot of ingredients, so I generally make enough for 2-3 servings at least. This recipe yields 36 oz, enough for two meals and one snack.
Black Forest Bliss Smoothie:
1 cup milk of your choice
1/2 head red kale
6 oz frozen cherries (a little over 1/2 a 10 oz package)
1/2 cup frozen raspberries
1/3 of a medium banana (enough to add texture and flavor, not enough to make the smoothie a sugar factory)
3 scoops chocolate protein powder
3 tbls cacao powder
1 tbls coconut oil
1-2 droppers chocolate-raspberry stevia
1/2 tsp Himalayan salt
In the VitaMix, prior to blending